Indirect organogenesis for high frequency shoot regeneration of two cultivars of Sansevieria trifasciata Prain differing in fiber production

Sansevieria trifasciata is used as an indoor plant, in traditional medicine and as a fiber source. Here we characterized fibers of two of varieties of S. trifasciata, Lorentii and Hahnii, and report a protocol for their propagation based on indirect shoot organogenesis. Structural and ribbon fibers were scattered within leaf parenchyma when viewed with confocal laser scanning microscopy. Chemical analysis of the fibers by mass spectrometry and high-performance chromatography revealed higher contents of cellulose and xylose in Lorentii than in Hahnii and significant differences for total lignin between both. A protocol for de novo shoot production was then developed using leaf explants. Time-course histological analyses showed that the first events of transdifferentiation were triggered preferentially in cells surrounding fibers and vascular bundles. Callogenesis and shoot performances were quantified for both varieties, and 2,4-D at 2 and 3 mg·L-1 yielded the best results for primary calli induction and fresh calli mass. The length, number, and mass of shoots produced did not differ significantly between the two cultivars. The fast morphogenic response of S. trifasciata to in vitro culture may be useful for mass propagation or other biotechnological purposes such as metabolite production.


Results and discussion
Contrasting leaf morphology and fiber traits of cvs Lorentii and Hahnii. Because Sansevieria species have an acaulescent-type growth, here plant height was determined by measuring the length of a fully developed adult leaf. Lorentii plants are 4.6 times taller than Hahnii plants; however, they have fewer leaves (Fig. 1a,b). Consistent with a leaf-dependent plant size, leaf area and fresh/dry mass were significantly greater in Lorentii than in Hahnii (Fig. 1c,d). The results of our morphological characterization of Hahnii are similar to those of tropical dwarf accessions of Sansevieria with sizes that range from 8.59 to 12.08 cm 26 . A small size is a key advantage for a model plant species 27,28 . An emerging model for Crassulacean acid metabolism (CAM) plants is Kalanchoë daigremontiana 29 , a species with a height up 1 m. Sansevieria species, especially its dwarf accessions, may be considered as an alternative option for the study of CAM.
We then examined the morphology of the fibers in leaf cross sections from the two cultivars (Fig. 2a). Two types of fibers were found in both cultivars. Structural fibers were composed of sclerenchyma cells with thickened secondary cell walls that formed polyhedral fiber bundles distributed in peripheral rows in the abaxial and adaxial sides of leaves (Fig. 2b,c). In Lorentii, structural fibers were found as bundles of up to 150 cells. In contrast, in Hahnii, these types of fiber bundles had fewer cells, especially in the abaxial leaf side (≤ 29 cells) (Fig. 2c). Ribbon or arc fibers, scattered in the middle part of the ground tissue of the leaves of both cultivars, had a two-dimensional vascularization pattern as described for succulents 30 (Fig. 2b). Ribbon fibers form a cap surrounding the vascular bundles; in Lorentii, these caps have up to 93 cells and up to 25 cells in Hahnii. In both cases, ribbon fibers are perivascular sclerenchyma fibers that protect the phloem but are never close to the vascular bundle (Fig. 2c). This fiber morphology for S. trifasciata is consistent with that reported for S. cylindrica 31 . The variations found in the morphology of structural fibers in the two cultivars of Sansevieria analyzed here may be associated with differential development of the parenchyma in unifacial or bifacial leaves, which has been previously observed for Asparagales species, including Sansevieria 32,33 . More studies on the biomechanics and functional morphology will be required to know whether and how unifacial (S. cylindrica) or bifacial development (S. trifasciata) affects the distribution of structural fibers that are thought to provide stiffness to leaf blades in monocots.
Imaging of cellulose and lignin in Sansevieria fibers by laser confocal scanning microscopy showed differences between both cultivars analyzed (Fig. 2c). Thus, we quantified the levels and composition of cell wall components in the fibers of Lorentii and Hahnii (Table 1). Cellulose, a homopolymer of glucose monomers, was the major constituent in Sansevieria fibers, encompassing up to 41.2% of the dry mass in Lorentii fibers. Lorentii fibers had 1.25 times more cellulose than did Hahnii fibers. For the hemicellulose fraction, xylose was the most abundant monosaccharide in both cultivars, accounting for 11.2% and 8.7% of the dry mass in Lorentii and Hahnii fibers, respectively. Significant amounts of arabinose (up 0.34%) and mannose (0.33%) were also found, especially in cv Hahnii (Table 1). In the evaluation of lignin composition in the raw fibers, the lignin autofluorescence analysis suggested significant differences in lignin content between the Sansevieria accessions, which were confirmed by pyrolysis molecular beam mass spectrometry (py-MBMS) ( Table 1). The fibers in both cultivars were rich in S-lignin, with contents of the carbohydrate fraction (C5 including xylan and other hemicellulose sugar, and C6 like glucan and cellulose) and total lignin estimated at 1% and 14% of dry mass, respectively (Table 1). Cellulose level obtained here (41.2%) for the two cultivars of S. trifasciata was lower than previously reported for S. trifasciata (56%), S. cylindrica (79.7%), S. ehrenbergii (80%) and S. roxburghiana (78.63%) 31,[34][35][36] . In contrast, lignin content was higher in our study compared with a previous analysis of S. trifasciata fibers that showed that Klason lignin made up 6% of the total dry mass 34 , about 42% lower than we found by py-MBMS. The differences in lignin composition may be due to differences in the type of lignin quantified in each technique (Klason lignin, acid-insoluble lignin; pyMBMS, total lignin) and sensitivity of the methods used 37 . For Sansevieria fibers, our report is the first to determine the chemical composition using high performance chromatography and mass spectroscopy. Differences in the chemical composition and morphology of the fibers in the two cultivars examined here seem to support the classification of very-soft fiber accession reported for S. trifasciata cv. Golden Hahnii 38 and may account for differences in thermal and mechanical properties, which have so far been analyzed for Lorentii but not Hahnii 1,39,40 . In S. cylindrica, the fibers have slightly lower cellulose and hemicellulose contents and a 50% less lignin than in S. ehrenbergii, which causes notable differences in the density, tensile strength, Young's modulus and elongation at break values of the fibers (reviewed by Lokantara et al. 41 ). As lignin levels were similar in Lorentii and Hahnii analyzed here, potential differences in fiber tensile strength between cvs could be explained by differences in the cellulose and xylose contents found (Table 1). More research is necessary to support this hypothesis.
Lorentii and Hahnii differ in morphogenic responses to in vitro culture. To assess and compare the morphogenic response to in vitro culture of cvs Lorentii and Hahnii, we optimized an indirect organogenesis protocol for shoots ( Supplementary Fig. 1), characterizing the initiation of organogenesis and the yields in each phase from callus induction to shoot production. An overview of these different phases is illustrated in Fig. 3. For both cultivars, primary callus was obtained from leaf segments after 42 days incubation (dai) in Murashige & Skoog 42 (MS) medium supplemented with 2,4-D ( Fig. 3a-e, j-n). The calli were friable and white-cream in color (Fig. 3e,n), typical of healthy, embryonic-like calli of monocots [43][44][45][46] . Although most chlorophyll content was lost and calli were already visible after 14 dai, 1 week earlier than previously reported for S. trifasciata 47  www.nature.com/scientificreports/ the mesophyll tissue and exclusively surrounding vascular bundles and ribbon fiber caps (Fig. 4). These structures developed faster in cv Hahnii than in cv Lorentii. At 14 dai, the cell clusters had increased in volume and almost broke through the leaf epidermis ( Fig. 4), explaining previous observations of calli located at the edges of Sansevieria leaf segments 47 . At the last time sampled, cell clusters also surrounded the structural fibers in both cultivars ( Supplementary Fig. 2). In vitro cultured, leaf-derived calli can have different forms of ontogenesis. For example, in the woody monocot Phoenix dactylifera, calli are formed from fascicular parenchyma cells or perivascular sheath cells (PSCs) depending on the differentiation grade of the leaf explant used 48 . In Coffea arabica, a pro-embryogenic mass and callus originate from mitotically active cells found near vascular bundles 49 . Similarly in our study, Sansevieria leaf calli seem to derive exclusively from PSCs or totipotent cells surrounding fibers (sclerenchyma). PSCs may be considered pericycle-like cells, which are thought to serve as pluripotent stem cells for callus initiation and shoot organogenesis 50,51 , similarly to that observed in our results. In the case of the calli that formed around Sansevieria structural fibers, we presume they may be derived from remnant cells of the ground meristem, which is known to give rise to such extraxylary fibers 52 . Callogenesis performance of the two Sansevieria cultivars in response to four doses of 2,4-D (1, 2, 3, and 4 mg·L -1 ) was also assessed. By 42 days after treatment, callus induction for both cultivars showed a clear dose response (Fig. 5A). The doses most effective for inducing callus were 2 and 3 mg·L -1 , but the highest dose reduced induction by 7.8% in Lorentii and 12.2% in Hahnii compared to the highest induction values obtained. In addition, Hahnii was more sensitive to 2,4-D (Fig. 5a). Our results for callogenesis induction are in line with previous reports for other monocot species such as agave, sugar cane, coconut, sorghum and desho; very high doses of 2,4-D considerably inhibited callus induction 45,[53][54][55][56] .
The calli induced by the two most efficient doses were then weighed, calli areas calculated, and the gains obtained using the initial and final values for both parameters. After 6 weeks of treatment, in both cultivars, the callus mass and area under the two doses were similar in both snake varieties (Fig. 5b,d) (Table S1, S2). It is worth mentioning high gains in biomass and area during callogenesis of both Sansevieria cvs during short treatment time (Fig. 5c,e) (Table S1, S2). This high efficiency of callogenesis in snake plant is similar to that observed in Campomanesia adamantium 57 . In monocots, callogenesis performance has been quantified for only a few plant species so far. For example, in Hyacinthus orientalis up to 0.9 g callus/explant from leaf tissue was obtained after 6 weeks of culture on MS medium supplemented with 2 mg·L -1 of BAP and 1 mg·L -1 of kinetin 58 , whereas Zingiber officinale yielded up to 3.89 g of callus/g explant from leaf tissue after 30 days on MS medium with 2 mg·L -1 of 2,4-D and 1 mg·L -1 of BAP 59 . Although the callus induction conditions used for these two monocot species and those we evaluated here differ, the callogenesis performance obtained for S. trifasciata is outstanding; rapid cell transdifferentiation may conduct to high yields of callus biomass. This behavior of snake plants during callogenesis may be helpful for establishing cell cultures for biotechnological purposes using the method described here. www.nature.com/scientificreports/ For de novo shoot production, the primary calli were transferred to 1X MS medium supplemented with 4.0 mg·L -1 of BAP. After 4 weeks, primary calli produced chlorophyll and became organogenic. The indices of organogenic callus production for cvs Lorentii and Hahnii did not differ significantly (Fig. 6a) (Table S3). Shoots emerged after 8 weeks and were maintained in these conditions until week 12. Hahnii produced about 1.5 times more shoots than Lorentii (Fig. 6B) (Table S3), thus positively affecting the shoot production index calculated for both cultivars (Fig. 6c). When the length, fresh and dry mass of the shoots were compared between the two cultivars, no significant differences were found (Fig. 6d-f) (Table S3). Shoot production rates quantified here for both Lorentii and Hahnii were up to 4 times lower than reported for the same varieties previously 24 and similar to that found by Hematharshini and Seran 50 , but faster than in both previous reports (4 weeks sooner). Our data suggest Hahnii is a cultivar with a stronger response to de novo shoot production than Lorentii, contradictory to the report of Yusnita et al. 24 .
Snake plants are also recognized for their rapid root production during conventional propagation using rhizomes or adult leaf cuttings 25,49,61 , suggesting that levels of endogenous auxins are sufficient for rhizogenesis. During the development of our protocol for in vitro multiplication, we observed that leaf explants on basal 1X MS medium yielded a higher frequency of root induction from Hahnii (63.3%) compared to Lorentii (12.2%) (Fig. 7a). Similarly, at the in vitro rooting stage, roots were generated when shoot cultures were grown with 4.0 mg·L -1 of BAP, without exogenous auxins, for both cultivars (Fig. 7b-e). Moreover, the root system was well-developed on plantlets grown in a hormone-free basal 1X MS medium (Fig. 7f-h). This last phase of our micropropagation protocol, an exogenous auxin-free rooting, contrast with those of Hematharshini and Seran 60 and Simbolon 61 , who used 0.5 mg·Lˉ1 of NAA and 2.0 mg·L -1 of BAP to produce shoots and roots, respectively, and those of Kaur 25 , who used high doses of IBA (5.0-10.0 mg·L -1 ), and Sarmast et al. 22 and Wahyuningsih et al. 62 , who immersed shoots for 3 s in an IBA solution (2000 mg·L -1 ), to induce rooting.

Conclusions
To sum up, morphological and chemical characterization of fibers of two cultivars of S. trifasciata, Lorentii and Hahnii, was carried out. Histological analysis revealed a similar distribution pattern of structural and ribbon fibers in both cultivars but differences in their chemical composition. Lorentii showed higher cellulose and xylose contents than Hahnii, while the lignin levels were similar. These differences found may explain the different strength properties previously known for both cvs. Snake plants were also efficiently propagated using an indirect organogenesis protocol. The protocol proposed takes only 140 d from leaf explant to plantlets. Time-course histological analysis revealed early transdifferentiation events occurring around vascular bundles, which lead to a high organogenic callus production. Dosis-responses analysis showed that 2 and 3 mg·L-1 of BAP were the most efficient doses for callus induction, with performance levels similar in both cvs. When shoot production was characterized, Hahnii showed a stronger response to de novo shoot production than Lorentii. Our results showed S. trisfasciata can be easily and efficiently propagated via indirect organogenesis.  www.nature.com/scientificreports/ terized by counting all leaves and measuring the length, width, area, fresh and dry mass of three fully expanded leaves.

Leaf morphometry and fiber chemical characterization. Cultivars Lorentii and Hahnii of
For fiber characterization, adult leaves were autoclaved (121 °C, 15 PSI, 20 min), then the fibers were extracted manually using sharp tweezers, washed with tap water, and dried at 65 °C for 3 days. For monosaccharide composition fibers were processed as reported previously 48 . Fibers were freeze-dried overnight, ground and soaked in chloroform-methanol (2:1) for 1 h, then twice each in 70% ethanol for 1.5 h, 80% ethanol for 1 h, and 95% ethanol for 2 h at room temperature. Treated fibers were briefly washed with acetone and dried under a stream of air. For removing any residual starch during sampling, fibers were incubated with pancreatic α-amylase (16 U/g) (Sigma-Aldrich, Germany) overnight, and washed with acetone. Monosaccharides were obtained by Saeman hydrolysis; fibers were placed in 72% sulfuric acid for 3 h at room temperature, then the acid solution was diluted to 6% with deionized water and incubated at 100 °C for 3 h. Inositol was added to all samples as an internal standard before the acid hydrolysis. All hydrolysates were filtered through 0.2 µm nylon syringe filters,  www.nature.com/scientificreports/ then analyzed using high performance anion exchange chromatography with pulsed amperometric detection (HPAEC-PAD) (ICS-3000, Dionex, Thermo Fisher Scientific, Sunnyvale, USA) equipped with a CarboPac PA1 column (4 × 250 mm, Dionex) as previously reported 50 .
For lignin composition (total lignin and monolignols), fiber samples were analyzed by pyrolysis-molecular beam mass spectrometry (py-MBMS) as reported previously 63,64 . Samples (1.5 to 3.0 mg) were prepared in duplicate; each was placed into a stainless metal cup, and single-shot pyrolyzed (Frontier Lab) at 500 °C to produce volatile compounds. The volatile compounds were analyzed for lignin using a molecular beam mass spectrometer (Extrel Core Mass Spectrometers). The raw data were processed through UnscramblerX 10.1 software to obtain the main components and raw lignin data. Also, NIST 8492 (lignin content, 26.2%) and Aspen standards were pyrolyzed and analyzed in the same manner and in the same batch as the unknown samples. Both standards were used for data quality control. Additionally, NIST 8492 was used to correct the raw lignin data.
In vitro culture establishment. For in vitro culture, long strips of leaf segments were cut from the central midsection of fully expanded leaves. These leaf segments were hand-washed with running tap water and ordinary liquid soap for 10 min and then washed for 5 min with running water. In a laminar flow hood, they were then immersed for 10 min in 20% (v/v) commercial bleach (containing 5.25% sodium hypochlorite), followed by 1 min in 70% (v/v) ethanol. Next, they were soaked in an aqueous solution of cefotaxime 250 mg·L -1 and carbenicillin 50 mg·L -1 for 15 min. Finally, an axenic culture was established as follows: small leaf segments (0.5-1 cm 2 ) were placed in Petri dishes that contained 25 mL of 1X MS medium (Caisson Labs) supplemented with 250 mg·L -1 cefatoxime, 3% (w/v) sucrose, 0.65% (w/v) agar (Micropropagation Agar Type I, Caisson Labs), and pH adjusted to 5.8 with KOH. The dishes were then incubated at 28 ± 2 °C with cool white LED lights (40 μmol m -2 s -1 ) and a 16 h light:8 h dark cycle. www.nature.com/scientificreports/ Callus induction. Small leaf segments (0.5-1 cm 2 ) from plantlets cultured as previously reported 24 were placed with the adaxial leaf side down on 1X MS agar prepared as described above but without antibiotics. For callus induction, 2,4-dichlorophenoxyacetic acid (2,4-D) (Caisson Labs) was tested at 0, 1, 2, 3, and 4 mg·L -1 . For all treatments (completely randomized design, three replicates per treatment, 10 explants per replicate), plates were incubated as described above. Callus induction percentage was quantified after 6 weeks of culture.
To determine the in vitro callogenesis performance for each cultivar of S. trifasciata, a second experiment (three replicates per treatment, 16 explants per replicate) was established using 2 and 3 mg·L -1 of 2,4-D doses, the best performing doses based on data from the callus induction experiment. Callus induction percentage, fresh callus mass and callus area were evaluated. For calculating callus area, calli were photographed and the calli areas were obtained using the free ImageJ software (NIH, US). Initial (IV) and final values (FV) of mass and area were then used to obtain gain values after treatment (Gain = FV-IV).
De novo shoot organogenesis. For organogenic callus (OC) production, 6-week-old primary calli of both Sansevieria cultivars were transferred to 1X MS medium supplemented with BAP (4.0 mg·L -1 ) (Caisson Labs), 3% (w/v) sucrose, 0.65% (w/v) agar (Micropropagation type I, Caisson Labs), and pH adjusted to 5.8 with KOH. The BAP dosis used was selected according preliminary experiments for shoot proliferation in our laboratory and previous reports 65 . Incubation conditions were as described above. For each cultivar, five replicates were used per treatment with 16 explants per replicate in a completely randomized design. After 4 weeks, the capacity of OC production was determined by calculating the OC production index (fresh OC mass/fresh mass of primary callus). For de novo shoot formation, OC were subcultured for another 8 weeks in the same culture medium and incubated as described. To compare shoot production by each cultivar, we evaluated shoot number/ callus, shoot production index (shoot number/fresh OC mass), shoot length, and fresh and dry shoot masses.
Histological analysis. Transdifferentiation events during callus induction with 2 mg/L of 2,4-D, the best performing treatment according to the dose-response experiment described above, were examined microscopically in leaf samples collected at 2, 4, 7, and 14 days after the start of treatment. Samples were placed immediately in 4% paraformaldehyde (Sigma-Aldrich) (w/v) in 1X phosphate-buffered saline solution, and fixed at 4 °C for www.nature.com/scientificreports/ 1 week. The fixed tissues were then dehydrated in ethanolic series (30,50,70, 85, 96 and 100%) (2 h twice for each) at room temperature. Samples were embedded using an epoxy medium (JB-4, Polysciences) according to the manufacturer's specifications. Resin-embedded samples were sectioned (8-10 µm thick) using an automatic rotatory microtome (Leica RM2255). Cross sections were stained using a 1:1 aqueous solution of 1% w/v methylene blue and 1% w/v azure B 66 for 20 s at room temperature and washed with distilled water, dried at 50ºC overnight and mounted in synthetic resin (Hycel, 7987). Leica DM2000 and Carl Zeiss Axioakop 2 Plus microscopes were used for imaging the stained sections. Lignin and cellulose were analyzed by confocal laser scanning microscopy (Leica TCS SP8). Lignin was detected by autofluorescence (405 nm excitation, 414-501 nm emission) and cellulose was detected by staining with an aqueous solution of propidium iodide (10 mg mL -1 ) (Sigma-Aldrich, Germany) (488 nm excitation, 642-748 nm emission).
Statistical analyses and image processing. All data, reported as means ± standard deviations (SD), were analyzed as a completely randomized factorial design. One-way independent ANOVA analyses were carried out using SAS software v. 9.2 (SAS Institute, Cary, NC, USA). For comparisons between treatments, Tukey's honestly significant difference (HSD) tests were performed (p ≤ 0.05). Figures were prepared using Remove. bg (Kaleido Al GmbH, Vienna, Austria), PowerPoint (Microsoft, Redmond, USA) and iLovePDF (PDF-Tools, Barcelona, Spain).

Data availability
All data generated or analyzed during this study are included in this published article [and its supplementary information files]. www.nature.com/scientificreports/